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Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices

Heart failure with preserved ejection fraction (HFPEF) is characterized by myocardial interstitial fibrosis. A total of 146 patients with HFPEF, were recruited. HFPEF severity was determined using Doppler imaging (E/Em) and also cardiac magnetic resonance imaging (CMRI). Canine modeling of HFPEF was...

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Autores principales: Wu, Cho-Kai, Su, Mao-Yuan, Lee, Jen-Kuang, Chiang, Fu-Tien, Hwang, Juey-Jen, Lin, Jiunn-Lee, Chen, Jin-Jer, Liu, Fu-Tong, Tsai, Chia-Ti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652206/
https://www.ncbi.nlm.nih.gov/pubmed/26582585
http://dx.doi.org/10.1038/srep17007
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author Wu, Cho-Kai
Su, Mao-Yuan
Lee, Jen-Kuang
Chiang, Fu-Tien
Hwang, Juey-Jen
Lin, Jiunn-Lee
Chen, Jin-Jer
Liu, Fu-Tong
Tsai, Chia-Ti
author_facet Wu, Cho-Kai
Su, Mao-Yuan
Lee, Jen-Kuang
Chiang, Fu-Tien
Hwang, Juey-Jen
Lin, Jiunn-Lee
Chen, Jin-Jer
Liu, Fu-Tong
Tsai, Chia-Ti
author_sort Wu, Cho-Kai
collection PubMed
description Heart failure with preserved ejection fraction (HFPEF) is characterized by myocardial interstitial fibrosis. A total of 146 patients with HFPEF, were recruited. HFPEF severity was determined using Doppler imaging (E/Em) and also cardiac magnetic resonance imaging (CMRI). Canine modeling of HFPEF was induced by aortic banding. Hemodynamic and echocardiographic data were obtained before and after pressure loading and myocardial Galectin-3 was determined. Mechanical stretch of cultured cardiomyocytes served as the cellular model of HFPEF. Patients with severe HFPEF had significantly higher plasma Galectin-3 levels. Significant correlation between plasma Galectin-3 and E/Em in advanced HFPEF patients was noted. After 2 weeks of pressure overload in canine models, the protein expression of Galectin-3 from LV myocardial tissue was significantly increased (p < 0.01) compared with controls. Galectin-3 expression paralleled the severity of LV diastolic dysfunction by evaluation of CMRI (r = −0.58, p = 0.003) and tissue fibrosis (r = 0.59, p = 0.002). After adjusting for confounders for diastolic dysfunction, Galectin-3 levels were still associated with diastolic parameters both in humans (p < 0.001) and canine model (p = 0.041). Mechanical stretch increased Galectin-3 secretion in cultured cardiomyocytes. Both plasma and myocardial Galectin-3 levels correlated with severity of cardiac diastolic dysfunction.
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spelling pubmed-46522062015-11-24 Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices Wu, Cho-Kai Su, Mao-Yuan Lee, Jen-Kuang Chiang, Fu-Tien Hwang, Juey-Jen Lin, Jiunn-Lee Chen, Jin-Jer Liu, Fu-Tong Tsai, Chia-Ti Sci Rep Article Heart failure with preserved ejection fraction (HFPEF) is characterized by myocardial interstitial fibrosis. A total of 146 patients with HFPEF, were recruited. HFPEF severity was determined using Doppler imaging (E/Em) and also cardiac magnetic resonance imaging (CMRI). Canine modeling of HFPEF was induced by aortic banding. Hemodynamic and echocardiographic data were obtained before and after pressure loading and myocardial Galectin-3 was determined. Mechanical stretch of cultured cardiomyocytes served as the cellular model of HFPEF. Patients with severe HFPEF had significantly higher plasma Galectin-3 levels. Significant correlation between plasma Galectin-3 and E/Em in advanced HFPEF patients was noted. After 2 weeks of pressure overload in canine models, the protein expression of Galectin-3 from LV myocardial tissue was significantly increased (p < 0.01) compared with controls. Galectin-3 expression paralleled the severity of LV diastolic dysfunction by evaluation of CMRI (r = −0.58, p = 0.003) and tissue fibrosis (r = 0.59, p = 0.002). After adjusting for confounders for diastolic dysfunction, Galectin-3 levels were still associated with diastolic parameters both in humans (p < 0.001) and canine model (p = 0.041). Mechanical stretch increased Galectin-3 secretion in cultured cardiomyocytes. Both plasma and myocardial Galectin-3 levels correlated with severity of cardiac diastolic dysfunction. Nature Publishing Group 2015-11-19 /pmc/articles/PMC4652206/ /pubmed/26582585 http://dx.doi.org/10.1038/srep17007 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wu, Cho-Kai
Su, Mao-Yuan
Lee, Jen-Kuang
Chiang, Fu-Tien
Hwang, Juey-Jen
Lin, Jiunn-Lee
Chen, Jin-Jer
Liu, Fu-Tong
Tsai, Chia-Ti
Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
title Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
title_full Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
title_fullStr Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
title_full_unstemmed Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
title_short Galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
title_sort galectin-3 level and the severity of cardiac diastolic dysfunction using cellular and animal models and clinical indices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652206/
https://www.ncbi.nlm.nih.gov/pubmed/26582585
http://dx.doi.org/10.1038/srep17007
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